Protein Xpc

URN urn:agi-llid:7508
Connectivity 89
Name Xpc
Description xeroderma pigmentosum, complementation group C
Notes This gene encodes a component of the nucleotide excision repair (NER) pathway. There are multiple components involved in the NER pathway, including Xeroderma pigmentosum (XP) A-G and V, Cockayne syndrome (CS) A and B, and trichothiodystrophy (TTD) group A, etc. This component, XPC, plays an important role in the early steps of global genome NER, especially in damage recognition, open complex formation, and repair protein complex formation. Mutations in this gene or some other NER components result in Xeroderma pigmentosum, a rare autosomal recessive disorder characterized by increased sensitivity to sunlight with the development of carcinomas at an early age. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq]

Pathway nucleotide excision repair pathway
altered nucleotide excision repair pathway

GO Molecular Function DNA binding
damaged DNA binding
single-stranded DNA binding

GO Cellular Component cytoplasm
nucleoplasm
nucleus

GO Biological Process cell cycle checkpoint
intra-S DNA damage checkpoint
DNA repair
nucleotide-excision repair
nucleotide-excision repair, DNA damage removal
response to DNA damage stimulus
response to drug
response to UV-B

Ariadne Ontology DNA repair

Group DNA repair
cell cycle checkpoint
intra-S DNA damage checkpoint
DNA repair
nucleotide-excision repair
nucleotide-excision repair, DNA damage removal
response to DNA damage stimulus
response to drug
response to UV-B
DNA binding
damaged DNA binding
single-stranded DNA binding
cytoplasm
nucleoplasm
nucleus

MedScan ID 7508

Hugo ID 12816

Human chromosome position 3p25

LocusLink ID 7508
22591
312560

Alias XP3
RAD4
XPCC
DNA repair protein complementing XP-C cells
p125
DNA repair protein complementing XP-C cells homolog
OTTMUSP00000028684
xeroderma pigmentosum group C-complementing protein homolog
xeroderma pigmentosum, complementation group C
DNA-repair protein complementing XP-C cells
Xeroderma pigmentosum group C complementing protein
xeroderma pigmentosum group c protein
xeroderma pigmentosum, complementing group C
XPC

Organism Homo sapiens
Mus musculus
Rattus norvegicus

GenBank ID NC_000003
NR_027299
NM_004628
NP_004619
NM_001145769
NP_001139241
NT_022517
NW_001838877
NW_921651
NG_011763
AC_000135
AC_000046
AC093495
AF261901
AAF87574
AY131066
AAM77801
CH471055
EAW64188
EAW64189
FJ695191
FJ695192
AI091587
AK222844
BAD96564
AK289761
BAF82450
AK295711
BAG58555
AK311039
AL710884
BC016620
AAH16620
CR615074
D21089
BAA04651
EU530523
ACD74564
EU530524
ACD74565
EU530525
ACD74566
EU530526
ACD74567
EU530527
ACD74568
EU530529
ACD74569
EU530532
ACD74571
EU530534
ACD74573
HM113488
ADI50189
X65024
CAA46158
Q01831
NC_000072
NM_009531
NP_033557
NT_039353
NW_001030811
AC_000028
AC161456
CH466523
EDK99303
AB071144
BAB64540
AK004713
BAB23497
AK028595
BAC26023
AK166981
BAE39163
AK170975
BC052725
AAH52725
BY238377
DV645509
U27398
AAC52500
U40005
AAA82720
P51612
Q7TSZ1
NC_005103
NM_001107874
NW_001084830
NW_047695
AC_000072
CH473957
EDL91370

OMIM ID 613208
278720

Mouse chromosome position 6

GO ID 0003684
0003697
0006281
0000075
0031573
0006289
0000718
0010224
0005654
0005634
0003677
0006974
0005737
0042493

Rat chromosome position 4q34

Swiss-Prot Accession B4DIP3
Q01831
P51612
Q7TSZ1
Q53GT7
Q96AX0
P54732
Q3TKI2
Q920M1
Q9DBW7

PIR ID S44345
S70630

Unigene ID Hs.475538
Mm.2806
Rn.22820

KEGG ID hsa:7508
mmu:22591
rno:312560

Swiss-Prot ID XPC_HUMAN
XPC_MOUSE
B4DIP3_HUMAN

Cell Localization Nucleus

IPI ID IPI00156793
IPI00124885
IPI00924991
IPI00794652
IPI00475584
IPI00365175

Homologene ID 3401

RGD ID 1305760

MGI ID 103557